A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22185



Internal ID15834823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376886..20384746hg38UCSC Ensembl
Outerchr15:20374150..20386258hg38UCSC Ensembl
Innerchr15:20582139..20589999hg19UCSC Ensembl
Outerchr15:20579403..20591511hg19UCSC Ensembl
Innerchr15:18842153..18850013hg18UCSC Ensembl
Outerchr15:18839417..18851525hg18UCSC Ensembl
Innerchr15:18842153..18850013hg17UCSC Ensembl
Outerchr15:18839417..18851525hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3812109
hg1912109
hg1812109
hg1712109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18537
Known Genes
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv22185
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer